首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >DETERMINATION OF LIQUIRITIN, GLYCYRRHIZIN, HESPERIDIN, CINNAMIC ACID, CINNAMALDEHYDE, HONOKIOL AND MAGNOLOL IN THE TRADITIONAL CHINESE MEDICINAL PREPARATION WUU-JI-SAN BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY
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DETERMINATION OF LIQUIRITIN, GLYCYRRHIZIN, HESPERIDIN, CINNAMIC ACID, CINNAMALDEHYDE, HONOKIOL AND MAGNOLOL IN THE TRADITIONAL CHINESE MEDICINAL PREPARATION WUU-JI-SAN BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY

机译:高效液相色谱法测定中药提取物五鸡三中中的皂苷,甘草甜素,橙皮苷,肉桂酸,肉桂醛,厚朴酚和甘露醇

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A high-performance liquid chromatographic method for the determination of liquiritin, glycyrrhizin, hesperidin, cinnamic acid, cinnamaldehyde, honokiol and magnolol in a traditional Chinese medicinal preparation, Wuu-Ji-San, which contains Glycyrrhizae Radix, Citri Leiocarpae Exocarpium, Aurantii Fructus, Cinniamomi Ramulus and Magnoliae Cortex, was established. The samples were separated with a Cosmosil 5C(18)-AR column by linear gradient elution using 0.03% (v/v) phosphoric acid-acetonitrile (0 min, 95:5; 52 min, 30:70) as the mobile phase at a how-rate of 1.0 ml/min and tile eluate was detected at 254 nn. n-Propyl benzoate was used as the internal standard and seven regression equations showing linear relationships between the peak-area ratios of each marker to n-propyl benzoate and concentration were obtained. The recoveries of the markers listed above were 84.77, 87.07, 79.81, 72.71, 72.72, 77.15 and 73.74%, respectively. The relative standard deviations were less than 5% (n=5). Very satisfactory and reproducible results were obtained within 52 min for the simultaneous determination of the seven markers. Different processes such as concentration by reduced-pressure evaporation, freeze-drying and spray-drying were studied with regard to their effects on the marker contents. There were only minor effects on most of the markers except cinnamic acid and cinnamaldehyde. Three commercial concentrated products of Wuu-Ji-San were also analysed. The contents of the marker substances in the commercial preparations were different from those in a standard decoction. [References: 10]
机译:一种高效液相色谱法,用于测定中药制剂Wuu-Ji-san中的甘草甜素,甘草甜素,橙皮苷,肉桂酸,肉桂醛,厚朴酚和厚朴酚,其中含有甘草基,柠檬皮,外皮,金桔成立了Cinniamomi Ramulus和Magnoliae Cortex。样品通过Cosmosil 5C(18)-AR色谱柱通过线性梯度洗脱进行分离,其中使用0.03%(v / v)磷酸-乙腈(0分钟,95:5; 52分钟,30:70)作为流动相。在254 nn处检测到1.0 ml / min的流速和瓷砖洗脱液。苯甲酸正丙酯用作内标,获得七个回归方程,这些方程显示了每种标记物与苯甲酸正丙酯的峰面积比与浓度之间的线性关系。上面列出的标记物的回收率分别为84.77、87.07、79.81、72.71、72.72、77.15和73.74%。相对标准偏差小于5%(n = 5)。在52分钟内获得了非常令人满意且可重复的结果,可同时测定7种标记物。研究了不同过程,如减压蒸发浓缩,冷冻干燥和喷雾干燥对标记物含量的影响。除肉桂酸和肉桂醛外,对大多数标记物仅有很小的影响。还分析了五极山的三种商业浓缩产品。市售制剂中标志物的含量与标准汤剂中的含量不同。 [参考:10]

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